Emergency research and the interests of participants
@article{Pattinson2012EmergencyRA,
title={Emergency research and the interests of participants},
author={S. Pattinson},
journal={Medical Law International},
year={2012},
volume={12},
pages={121 - 141}
}The UK Clinical Trials Regulations were amended in 2006 and 2008 to facilitate research on medicinal products administered in emergency situations. The Regulations, which implement the EU Clinical Trials Directive, had previously required prior consent to participation in a clinical trial from either the participant or the participant’s legal representative. These amendments put emergency research on medicinal products on a similar footing to research on other types of invasive emergency… CONTINUE READING
Top 3 of 3 Citations
Involving adults who lack capacity in research: ethical and legal challenges for the pre-hospital and emergency medicine context.
Non-beneficial pediatric research: individual and social interests
10
Rationale and design of: A Randomized tRial of Expedited transfer to a cardiac arrest center for non‐ST elevation out‐of‐hospital cardiac arrest: The ARREST randomized controlled trial
3
3 Citations
References
Publications referenced by this paper.
SHOWING 1-10 OF 18 REFERENCES
3A)(b)
3A)(c)